Canonical Allele Identifier: CA2290299505
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23845902C= , CM000680.2:g.23845902C= GRCh38
NC_000018.9:g.21425866C= , CM000680.1:g.21425866C= GRCh37
NC_000018.8:g.19679864C= NCBI36
NG_007853.2:g.161305C=

Transcript Alleles

HGVS Amino-acid change
ENST00000313654.14:c.3720-395C= MANE Select ENSP00000324532.8:n.3720-395C=
ENST00000649721.1:c.612-395C= ENSP00000497885.1:n.612-395C=
ENST00000313654.13:c.3720-395C= ENSP00000324532.8:n.3720-395C=
ENST00000399516.7:c.3720-395C= ENSP00000382432.2:n.3720-395C=
NM_001127717.2:c.3720-395C= NP_001121189.2:n.3720-395C=
NM_198129.2:c.3720-395C= NP_937762.2:n.3720-395C=
XM_011525978.1:c.3747-395C= XP_011524280.1:n.3747-395C=
XM_011525979.1:c.3738-395C= XP_011524281.1:n.3738-395C=
XM_011525980.1:c.3729-395C= XP_011524282.1:n.3729-395C=
XM_011525981.1:c.3615-395C= XP_011524283.1:n.3615-395C=
XM_011525982.1:c.3747-395C= XP_011524284.1:n.3747-395C=
XM_011525978.2:c.3747-395C= XP_011524280.1:n.3747-395C=
XM_011525979.2:c.3738-395C= XP_011524281.1:n.3738-395C=
XM_011525980.2:c.3729-395C= XP_011524282.1:n.3729-395C=
XM_011525981.2:c.3615-395C= XP_011524283.1:n.3615-395C=
XM_011525982.2:c.3747-395C= XP_011524284.1:n.3747-395C=
XM_017025743.1:c.1599-395C= XP_016881232.1:n.1599-395C=
XM_017025744.1:c.-905-395C= XP_016881233.1:n.-905-395C=
XR_001753199.1:n.3988-395C=
NM_001127717.3:c.3720-395C= NP_001121189.2:n.3720-395C=
NM_198129.3:c.3720-395C= NP_937762.2:n.3720-395C=
NM_001127717.4:c.3720-395C= NP_001121189.2:n.3720-395C=
NM_198129.4:c.3720-395C= MANE Select NP_937762.2:n.3720-395C=